@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_head
{
this:
np:hasAssertion
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_assertion
;
np:hasProvenance
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_assertion
a
np:Assertion
.
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_provenance
a
np:Provenance
.
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN86968dc8c7e3dce4add7f2c9699ee7b0
sio:SIO_000628
miriam-gene:2706
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_provenance
{
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_assertion
dcterms:description
"[This association emphasizes the need to consider Connexin 26 gene mutations in children who develop oral squamous cell carcinoma and to monitor for oral squamous cell carcinoma in children with Connexin 26 gene mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:20829717
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP636002.RArqiXmRhZj08H0GGHxYzEcPkQQIWWxQME040Tw_NJ3jQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}